Clinical Trial

Weaning From High Flow Nasal Oxygen in Acute Respiratory Failure : a Target Trial Emulation

Study acronym: HFNO-Weaning
Active, Not Recruiting
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Record status
This record was last updated August 8, 2025 (before its estimated September 30, 2025 completion). Its status may not reflect the trial's current state.
Summary
Acute respiratory failure is a frequent reason for admission to the intensive care unit (ICU). It is associated with high healthcare consumption and mortality. High-flow nasal oxygen (HFNO) improves comfort, reduces the risk of intubation and may reduce the risk of mortality in the most severe patients with acute hypoxemic respiratory failure compared with other oxygenation strategies. Therefore, HFNO is recommended as a first-line non-invasive oxygenation strategy in acute hypoxemic respiratory failure. The timing of weaning patients from HFNO is complex. On the one hand, failure to wean from HFNO is associated with prolonged duration of HFNO and prolonged ICU stay. On the other hand, continued HFNO in patients ready to be weaned may unnecessarily prolong ICU stay and contribute to overwhelming of ICU capacities. The overarching goal of this study is to identify the characteristics of patients in whom weaning from HFNO is not beneficial.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-06-12.
Status change: Completed → Active, Not Recruiting 2025-08-04
Trial Details
NCT Number NCT07030413
Lead Sponsor Poitiers University Hospital
Collaborators: University Hospital, Bordeaux, University Hospital, Limoges
Conditions Respiratory Failure With Hypoxia, Respiratory Failure, ICU, High-Flow Nasal Oxygen Therapy
Enrollment 2,000 participants
Start Date 2019-11-01
Primary Completion 2025-09-30 (estimated)
Study Completion 2025-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-08-08